Concept explainers
Interpretation:
The observation that Friedel-Crafts alkylations often give polysubstituted products but Friedel-Crafts acylations do not is to be explained.
Concept introduction:
Friedal-Crafts reaction is an electrophilic substitution reaction in which an
To explain:
The observations that Friedel-Crafts alkylation reactions give polysubstituted products but Friedel-Crafts acylations do not.
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Chapter 16 Solutions
Organic Chemistry
- Furan undergoes electrophilic aromatic substitution more readily than benzene; mild reagents and conditions are sufficient.For example, furan reacts with bromine to give 2-bromofuran. Explain why furan undergoes bromination (and other electrophilic aromatic substitutions) primarily at the 2-position.arrow_forwardThe following substances can be prepared by a nucleophilic addition reaction between an aldehyde or ketoneand a nucleophile. Identify the reactants from which they were prepared. If the substance is an acetal, identifythe carbonyl compound and the alcohol; if it is an imine or enamine, identify the carbonyl compound and theamine. You do not have to consider stereochemistry. In cases where there is more than one answer, just giveone. Use Grignard reagents when an organometallic reagent is required. Draw the Grignard reagent as acovalent magnesium bromide.arrow_forwardhelparrow_forward
- The carbocation electrophile in a Friedel-Crafts reaction can be generated in ways other than by reaction of an alkyl chloride with AlCl3. For example, reaction of benzene with 2-methylpropene in the presence of H3PO4 yields tert-butylbenzene. Draw a structure for the electrophile.arrow_forwardExplain briefly the reactivity of aldehydes and ketones toward nucleophilic reagentsarrow_forwardGeneral Features for Reaction of Organometallic Reagents withAldehydes and Ketones ?arrow_forward
- How does the reactivity of an aldehyde or a ketone toward nucleophiles compare with thereactivity of the carbonyl compounds whose reactions you studied in Chapter 15?arrow_forwardExplain why pyridine N-oxide G can undergo nucleophilic aromatic substitution with nucleophile Nuc– to give product I. Include the resonance structures of pyridine N-oxide G to illustrate your answer.arrow_forwardDemonstrate the results of the reactions between this alkyne and the various reagents.arrow_forward
- Use benzenonium resonance forms to explain why the methoxyl group (-OCH3) is o, p-directing in electrophilic aromatic substitution reactions.arrow_forwardUsing the concept of resonance, explain why the nitro group deactivates electrophilic aromatic substitution reactions, but facilitates nucleophilic aromatic substitution reactions.arrow_forwardExplain why pyridine N-oxide G can undergo electrophilic aromatic substitution with electrophile E+ to give product H. Include the resonance structures of pyridine N-oxide G to illustrate your answer.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning